Issue 3, 2019

Platinum(ii)-catalyzed selective para C–H alkoxylation of arylamines through a coordinating activation strategy

Abstract

A highly efficient method to selectively install alkoxy onto the para position of arylamines via a coordinating activation strategy has been reported. Various substrates are compatible, providing the corresponding products in good to excellent yields. This strategy gives an efficient and practical solution for the synthesis of unsymmetrical aryl ethers. A free radical pathway mechanism is advised for transformation.

Graphical abstract: Platinum(ii)-catalyzed selective para C–H alkoxylation of arylamines through a coordinating activation strategy

Supplementary files

Article information

Article type
Paper
Submitted
26 Nov 2018
Accepted
12 Dec 2018
First published
14 Dec 2018

Org. Biomol. Chem., 2019,17, 490-497

Platinum(II)-catalyzed selective para C–H alkoxylation of arylamines through a coordinating activation strategy

J. Shen, J. Xu, H. Cai, C. Shen and P. Zhang, Org. Biomol. Chem., 2019, 17, 490 DOI: 10.1039/C8OB02942C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements